23659-88-3 Usage
Uses
Used in Pharmaceutical Industry:
4,6-DiMethoxyindolin-2-one is used as a key intermediate in the synthesis of various pharmaceuticals, leveraging its unique structure and biological activities. Its anti-inflammatory and anticancer properties make it a promising candidate for the development of new drugs targeting these conditions.
Used in Agrochemical Industry:
4,6-DiMethoxyindolin-2-one is utilized as a building block in the creation of agrochemicals, contributing to the development of effective and environmentally friendly solutions for pest control and crop protection.
Used in Organic Electronic Devices:
4,6-DiMethoxyindolin-2-one is employed in the research and development of organic electronic devices, such as organic light-emitting diodes (OLEDs) and organic solar cells, due to its potential electronic properties and compatibility with organic materials.
Used in Organic Chemistry Research:
4,6-DiMethoxyindolin-2-one serves as a valuable precursor in the development of new synthetic methods and strategies in organic chemistry, enabling the exploration of novel chemical reactions and the synthesis of complex organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 23659-88-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,6,5 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 23659-88:
(7*2)+(6*3)+(5*6)+(4*5)+(3*9)+(2*8)+(1*8)=133
133 % 10 = 3
So 23659-88-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H11NO3/c1-13-6-3-8-7(5-10(12)11-8)9(4-6)14-2/h3-4H,5H2,1-2H3,(H,11,12)
23659-88-3Relevant academic research and scientific papers
A General Strategy for the Synthesis of 2,2'-, 2,3'-, and 2,7'-Bi-indolyls
Black, David St. C.,Kumar, Naresh
, p. 441 - 442 (2007/10/02)
Various substituted indoles undergo electrophilic substitution with indolin-2-one or 4,6-dimethoxyindolin-2-one and phosphoryl chloride to afford 2,2'-, 2,3'-, or 2,7'-bi-indolyls, depending on the initial substitution pattern.
